HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 15053185, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15053184 | HCID 15053184 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15053185 | HCID 15053185 | 78.8% |
Reaction Steps
To a solution of 8-(2-benzimidazolyl)thiomethyl-1-methyl-4-oxo-1,2,3,4-tetrahydroquinoline (300 mg) in methanol (10 ml) was added gradually sodium borohydride (35 mg) at 0° C. The reaction mixture was stirred for 40 minutes at room temperature. After distilling off the solvent, the resulting residue was extracted with dichloromethane, washed with water, and dried. Then the solvent was distilled off and the resulting residue was recrystallized from ethyl acetate-n-hexane to give 8-(2-benzimidazolyl)thiomethyl-1-methyl-4-hydroxy-1,2,3,4-tetrahydroquinoline (238 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963566 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-bfc36c35451343469e19d103192d3d22 |
| Source note | uspto-grants-1990_10 |